X–linked paroxysmal dyskinesia and severe global retardation caused by defective MCT8 gene
Year: 2005
Type: article
Study design: Case Report
Source: Journal of Neurology
Language: English
Subfield: Endocrinology, Diabetes and Metabolism
Field: Medicine
Domain: Health Sciences
Open Access status: closed
Awards: G1164413914, G3192969681
OpenAlex ID: W2013988137
